Scanning for lagging brainwaves could predict Alzheimer’s disease DECADES before memory loss starts, animal study suggests
- Scientists at the University of California, San Francisco, discovered that mice with an Alzheimer’s risk gene also have fewer ‘sharp-wave ripples’ in their brains
- These brainwaves are involved in learning and memory formation
- In new research, the scientists found that animals with fewer of those waves struggled with memory tasks months after the deficit was first detected
- Scans of the lagging brainwaves were first taken the equivalent of 30 years before memory loss would begin in a human
- The scientists say the findings may offer a non-invasive way to predict who will develop Alzheimer’s decades in advance
- Brainwave changes may also suggest a new target for treating symptoms involved in memory loss instead of underlying disease, they said
Alzheimer’s disease could be predicted by a brain scan – decades before symptoms develop, according to a new study.
Scientists have identified a type of brainwave that protects against the devastating neurological illness.
Known as sharp-wave ripple (SWR), it plays a direct role in spatial learning and memory formation in humans, mice and other mammals.
In experiments conducted by researchers at the University of California, San Francisco, lab rodents who lacked it performed worse on memory tasks 10 months later – the equivalent of 30 years for a human.
University of California, San Francisco researchers discovered a type of brainwave linked to an Alzheimer’s risk gene in 2016. Now, their new study in nice found that too few of the brainwaves predicts Alzheimer’s in animals the equivalent of 30 human years in advance
‘We were not betting on these results, the idea young mice with no memory problems already have the seed of what’s going to lead to deficits in old age,’ lead author Dr Emily Jones, of the University of California, San Francisco, said.
‘We would love to, but we thought it would be ridiculous to be able to predict so far in advance.’
Since SWRs are also found in humans the findings suggest they may serve as very early warning signs of dementia.
Senior author Dr Yadong Huang, who is based in the same lab, said: ‘A major advantage of this approach is that researchers have recently developed a noninvasive technique for measuring SWRs in people, without implanting electrodes in the brain,’
It could improve clinical trials testing new drugs to stave off Alzheimer’s. Enrolling patients who already show SWR deficits would enhance the results.
Measurements could also be taken repeatedly and non-invasively, enabling researchers to test drug effects over time, even before memory deficits appear.
One of the reasons medications have failed so far is they are given to participants too late – once symptoms have already taken hold.
Dr Huang said: ‘Being able to predict deficits long before they appear could open up new opportunities to design and test interventions that prevent Alzheimer’s in people.’
The findings published in Cell reports build on a 2016 study of mice engineered to carry a gene called ApoE4 (apolipoprotein E4) which increases the risk of Alzheimer’s in humans.
As they age, ApoE4 mice often develop signs of memory loss similar to those seen in patients.
SWRs occur when the brain of a resting mouse or human rapidly and repeatedly replays a recent memory of moving through a space, such as a maze or a house.
Dr Jones said: ‘SWRs have two important measurable components: abundance and short gamma (SG) power.
‘Broadly, SWR abundance predicts how quickly an ApoE4 mouse can learn and memorize how to get through a maze, and SG power predicts how accurate that memory will be.’
The earlier study revealed ageing ApoE4 mice have lower SWR abundance and weaker SG power than seen in healthy peers.
Dr Jones and colleagues reasoned measuring SWR activity could predict the severity of demonstrable memory problems in ApoE4 mice during ageing.
They first recorded SWR activity in these mice at rest. One month later, they had the mice perform spatial tasks to test their memory.
They found mice with fewer SWRs and lower SG power were indeed more likely to have worse spatial memory deficits.
‘We actually successfully replicated this experiment two years later with different mice,’ Dr Huang said.
‘What was striking is we were able to use the results from the first cohort to predict with high accuracy the extent of learning and memory deficits in the second cohort, based on their SWR activity.’
Even more striking were the unexpected results of the team’s next experiment. The researchers were curious how SWR activity evolves over a mouse’s lifetime.
So, they periodically measured SWRs in ApoE4 mice from an early age – long before memory deficits appeared – through middle age, and into old age.
Dr Jones said: ‘We thought that, if we got lucky, the SWR measurements we took when the mice were middle aged might have some predictive relationship to later memory problems.’
Surprisingly, the analysis revealed that deficits in SWR abundance and SG power at an early age predicted which mice performed worse on memory tasks – when they were much older.
Dr Huang says SWR directly measures the decline in brain function seen in Alzheimer’s – as opposed to a pathological change that only appears as a result of the underlying disease.
He added: ‘I feel strongly that Alzheimer’s research should not just focus on pathology, but use functional alterations like SWR deficits to guide research and drug development. Our new findings support this kind of approach.’
Alzheimer’s disease and other forms of dementia effects 850,000 people in the UK – a figure that will rise to 2 million by 2050. There is no cure.
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